| Tag | Content |
|---|
EnhancerAtlas ID | HS060-20448 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:191277920-191278870 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:191278336-191278357 | TGAGGAGGATAAAAAGGAGGA | + | 6.91 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I190413 | chr2 | 191278127 | 191278726 |
|
Enhancer Sequence | ACGTGTTGAT GATTATGTTG AAGAGATGTG AGTGAGAGTT CTGTATTACC TTGTGACCTG 60
GTGGTCCTGC TGCATTTTAG GATGGGAGGG GCGGGGTAGA ATGGGGGAGA ATAGGGCAAA 120
GATGGGAAGA AATTCAGACC CTTAAAAAAC CATGTTCAAG AGATGTGGAA AAAAATTGAA 180
TTAAGGGGGG CAGAGATGTC TTTCTTTGAC ATTTGTTGTG GGGCATGTTT TAGAATGGGA 240
GACCAATTCA GGAAACATTT GGCAAGTACA AAACAGGAAA GGCCAGCTCT GAATGACTCT 300
GAGGAAATGT TTGGAAGCAT TTTGATCTGA GACCAAGAGT GGGATGGGGG AAAGACAGGG 360
AAAGACAGGG ACACTATGAA TCAGCAGTGG GCAGAGTGAG CTCTGGTGTG TGGCTTTGAG 420
GAGGATAAAA AGGAGGAACT GGTGCTGCCT GAACAAGCCC GATGTGTGGG TTAACCGTGC 480
CAAAGGAAAG TGAGTGGCGA GCCTGGACTG GTAGTTAGCA GTCTGTGTTG GTTATGTAGA 540
GAGACCTTGT TCCACAGGCA GGTGCACTCC ACTCTGCACG GGGCCTGCTC TCTCTGAGCT 600
CCAATAAACC AATGTACCAT GAGCCCTGCT ATACTGTGGG GTGAAGAGGA GACATGGCAG 660
TCAGGGCCCA GGATTCCAGG AGAAACTGAG CACTGGAGCA GTGGCAGGAG TGGGTCCCTG 720
TGAGTCACGC TGGGAATTCT TAACTGTTCA GGGCACTTTT AGGGACAAAG TTAAGGTAGA 780
ACATACTTGG CCTCAAGGTA CTTGGCTCAA GGTAGAGCAA AGGAGGAAGG CACCACACCA 840
AACACATAAA GCAGAATCAT ACAAAGTGAC ATGCATGCTG CCTATGACTT TTAAGAAGTA 900
CTGTGTTCCT GGGGCCTGTC TGGGGGGTTG GGTGGCAGGG GGAGGGAGAG 950
|
